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199531009: Fetus with hereditary disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Aug 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
306590012 Fetus with hereditary disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
584171016 Fetus with hereditary disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011641019 Foetus with hereditary disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
306590012 Fetus with hereditary disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
306590012 Fetus with hereditary disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
584171016 Fetus with hereditary disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
584171016 Fetus with hereditary disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011641019 Foetus with hereditary disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3011641019 Foetus with hereditary disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4863061000241115 maladie héréditaire du foetus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4863061000241115 maladie héréditaire du foetus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fetus with hereditary disease Is a anomalie fœtale connue ou suspectée false Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease Occurrence Fetal period (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease Finding site Fetal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetus with hereditary disease Is a Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease Is a Foetal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Fetus with hereditary disease - delivered Is a False Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
fœtus avec problème prénatal et maladie héréditaire Is a False Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease unspecified Is a False Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Fetus with hereditary disease NOS Is a False Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Haemoglobin Bart's hydrops syndrome Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Bartter syndrome antenatal type 1 (disorder) Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Bartter syndrome antenatal type 2 (disorder) Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Hydrolethalus syndrome (disorder) Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Fetal cystic fibrosis Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Fetal encasement syndrome Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pontocerebellar hypoplasia type 12 Is a True Fetus with hereditary disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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